Adracalin 产品
(Achalasia, Adrenocortical Insufficiency, Alacrimia (AAAS))
Categories
The protein encoded by this gene is a member of the WD-repeat family of regulatory proteins and may be involved in normal development of the peripheral and central nervous system. The encoded protein is part of the nuclear pore complex and is anchored there by NDC1. Defects in this gene are a cause of achalasia-addisonianism-alacrima syndrome (AAAS), also called triple-A syndrome or Allgrove syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010].
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Featured Adracalin Categories
Adracalin 抗体
High quality antibodies with extensive validation data.
Adracalin ELISA试剂盒
Reliable ELISA kits for a wide range of species.
Adracalin 蛋白
Proteins for various applications incl. WB, ELISA, IF etc.
Recommended Adracalin 抗体
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ABIN2854764
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Recommended Adracalin ELISA试剂盒
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Recommended Adracalin 蛋白
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Latest Publications for our Adracalin Products
: "Nuclear pore heterogeneity influences HIV-1 infection and the antiviral activity of MX2." in: eLife, Vol. 7, (2019) (PubMed).Synonyms and alternative names related to Adracalin
aladin WD repeat nucleoporin (Aaas), achalasia, adrenocortical insufficiency, alacrimia (aaas), aladin WD repeat nucleoporin L homeolog (aaas.L), aladin WD repeat nucleoporin (AAAS), aladin WD repeat nucleoporin (aaas), achalasia, adrenocortical insufficiency, alacrimia (Aaas), AAA, AAASb, ADRACALA, ADRACALIN, aladin, Aladin, ALADIN, D030041N15Rik, GL003, zgc:85873Protein level used designations for Adracalin
- achalasia, adrenocortical insufficiency, alacrimia (Allgrove, triple-A)
- aladin
- Aladin
- achalasia, adrenocortical insufficiency, alacrimia
- aladin-like
- Allgrove, triple-A
- adracalin
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